[cite web | title = Entrez Gene: ULBP2 UL16 binding protein 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=80328| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Cerwenka A, Lanier LL |title=NKG2D ligands: unconventional MHC class I-like molecules exploited by viruses and cancer. |journal=Tissue Antigens |volume=61 |issue= 5 |pages= 335–43 |year= 2004 |pmid= 12753652 |doi=
*cite journal | author=Cosman D, Müllberg J, Sutherland CL, "et al." |title=ULBPs, novel MHC class I-related molecules, bind to CMV glycoprotein UL16 and stimulate NK cytotoxicity through the NKG2D receptor. |journal=Immunity |volume=14 |issue= 2 |pages= 123–33 |year= 2001 |pmid= 11239445 |doi=
*cite journal | author=Onda H, Ohkubo S, Shintani Y, "et al." |title=A novel secreted tumor antigen with a glycosylphosphatidylinositol-anchored structure ubiquitously expressed in human cancers. |journal=Biochem. Biophys. Res. Commun. |volume=285 |issue= 2 |pages= 235–43 |year= 2001 |pmid= 11444831 |doi= 10.1006/bbrc.2001.5149
*cite journal | author=Steinle A, Li P, Morris DL, "et al." |title=Interactions of human NKG2D with its ligands MICA, MICB, and homologs of the mouse RAE-1 protein family. |journal=Immunogenetics |volume=53 |issue= 4 |pages= 279–87 |year= 2001 |pmid= 11491531 |doi=
*cite journal | author=Sutherland CL, Chalupny NJ, Schooley K, "et al." |title=UL16-binding proteins, novel MHC class I-related proteins, bind to NKG2D and activate multiple signaling pathways in primary NK cells. |journal=J. Immunol. |volume=168 |issue= 2 |pages= 671–9 |year= 2002 |pmid= 11777960 |doi=
*cite journal | author=Radosavljevic M, Cuillerier B, Wilson MJ, "et al." |title=A cluster of ten novel MHC class I related genes on human chromosome 6q24.2-q25.3. |journal=Genomics |volume=79 |issue= 1 |pages= 114–23 |year= 2002 |pmid= 11827464 |doi= 10.1006/geno.2001.6673
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Dunn C, Chalupny NJ, Sutherland CL, "et al." |title=Human cytomegalovirus glycoprotein UL16 causes intracellular sequestration of NKG2D ligands, protecting against natural killer cell cytotoxicity. |journal=J. Exp. Med. |volume=197 |issue= 11 |pages= 1427–39 |year= 2003 |pmid= 12782710 |doi= 10.1084/jem.20022059
*cite journal | author=Rölle A, Mousavi-Jazi M, Eriksson M, "et al." |title=Effects of human cytomegalovirus infection on ligands for the activating NKG2D receptor of NK cells: up-regulation of UL16-binding protein (ULBP)1 and ULBP2 is counteracted by the viral UL16 protein. |journal=J. Immunol. |volume=171 |issue= 2 |pages= 902–8 |year= 2003 |pmid= 12847260 |doi=
*cite journal | author=Clark HF, Gurney AL, Abaya E, "et al." |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265–70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003
*cite journal | author=Eleme K, Taner SB, Onfelt B, "et al." |title=Cell surface organization of stress-inducible proteins ULBP and MICA that stimulate human NK cells and T cells via NKG2D. |journal=J. Exp. Med. |volume=199 |issue= 7 |pages= 1005–10 |year= 2004 |pmid= 15051759 |doi= 10.1084/jem.20032194
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Rohner A, Langenkamp U, Siegler U, "et al." |title=Differentiation-promoting drugs up-regulate NKG2D ligand expression and enhance the susceptibility of acute myeloid leukemia cells to natural killer cell-mediated lysis. |journal=Leuk. Res. |volume=31 |issue= 10 |pages= 1393–402 |year= 2007 |pmid= 17391757 |doi= 10.1016/j.leukres.2007.02.020
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